Author clinical study reports, protocols, informed consent forms, narratives, and investigator brochures across therapeutic areas.
Represent Medical Writing at meetings, drive document development, and articulate strategy and timelines.
Mentor junior staff, manage multiple priorities, and foster collaboration to resolve conflict.
Regeneron is a leading biotechnology company that invents life-transforming medicines for people with serious diseases. Founded and led for over 30 years by physician-scientists, the company has a fast-growing, science-driven culture and is recognized as a Great Place to Work in 2021, among other awards.
Leads writing and preparing clinical and regulatory documents for drug and device development.
Coordinates review, approval, and quality control across functions to ensure compliance and timelines.
Develops knowledge of US and international regulations and participates in process improvements.
AbbVie discovers and delivers innovative medicines and solutions addressing serious health issues in immunology, oncology, neuroscience, and aesthetics. They are a large global biopharmaceutical company committed to having a remarkable impact on people's lives.
Write clear and concise medical copy for HCPs and patients, adhering to ABPI guidelines and quality processes.
Collaborate with strategy, creative, and account teams to develop effective campaigns.
Manage projects from concept to completion, ensuring timelines and quality standards.
Real Chemistry is a global healthcare communications and marketing agency that partners with top pharmaceutical and biotech companies. The company fosters a culture of innovation and collaboration, with over 5 years of growth, and has been certified as a Great Place to Work.
Help build your dream AI-enabled authoring platform by guiding product and engineering teams on source data mapping, document logic, and summary execution.
Define document generation frameworks for regulatory-grade documents, starting with clinical trial results and scaling to broader submissions.
Establish objective quality criteria, review protocols, and verification frameworks to ensure outputs meet global regulatory expectations.
Veeva Systems is a mission-driven organization and pioneer in industry cloud, helping life sciences companies bring therapies to patients faster. As one of the fastest-growing SaaS companies in history, surpassing $3 billion in revenue, we are a public benefit corporation with a flexible work environment and a commitment to employee success.
Produce high-quality content for diverse medical communications projects, demonstrating excellent scientific understanding.
Develop content with minimal supervision, within budget and on time, using client approval systems.
Attend conferences, present work to clients, and manage day-to-day client communication and relationships.
Lumanity is dedicated to improving health outcomes by accelerating and optimizing access to life-changing medicines. As a global strategic partner, they bring together strategy, evidence, engagement, and technology to engineer breakthrough value.
Create high-quality medical affairs deliverables translating complex scientific data into clear, accurate content.
Collaborate with colleagues, clients, and external experts to shape audience-tailored materials aligned with client objectives.
Take ownership of projects from brief to delivery, ensuring scientific accuracy and engaging content.
Avalere Health is a healthcare agency focused on ensuring every patient is identified, treated, supported, and cared for. With major hubs in the US and UK, they emphasize inclusive culture, flexible work, and professional growth, supporting employee networks and family planning.
Develop medical affairs and publications content across multiple workstreams, ensuring high scientific quality and credibility.
Create materials tailored for different medical audiences with minimal internal review, demonstrating excellent quality control.
Collaborate with clients to ensure projects meet strategic marketing and medical needs, maintaining a client-centric attitude.
ApotheCom is a leader in medical communications, part of Inizio, a global healthcare consulting and communications group. With over 12,000 employees globally, Inizio creates compelling content and engages communities to achieve outcomes that matter.
Serving as medical point person on assigned accounts
Developing, writing and translating complex scientific data to a broad audience
Ensuring project quality and outcomes by demonstrating in-depth technical expertise
PRECISION AQ is a top payer marketing agency supporting global pharmaceutical and life sciences clients. The company offers training, mentorship, and a cross-functional project team environment.
Develop and review medical response documents with scientific accuracy and editorial excellence.
Perform source-to-output verification, validate references, and ensure consistency across deliverables.
Support MLR readiness through quality checks aligned with FDA guidance, AMA style, and ICMJE standards.
EVERSANA creates next-generation commercialization services for the life sciences industry. Their global team of over 6,000 employees serves more than 670 clients, from biotech start-ups to pharmaceutical companies, and embraces diversity and inclusion.
Manage and oversee all clinical aspects of trials across multiple countries, ensuring timeline adherence, quality, and scope.
Lead CRAs and collaborate with cross-functional teams to achieve high client satisfaction and smooth trial operations.
Identify risks, develop creative action plans, and maintain focus on study priorities through effective communication.
Precision for Medicine is a precision medicine CRO that combines novel trial designs, advanced biomarker analytics, and deep oncology expertise to accelerate drug development. The company fosters a dynamic, high-energy culture and values dedicated professionals who thrive in challenging environments.
Drive growth of Regulatory Science and Medical Writing services across pharmaceutical, biotechnology, and life sciences clients.
Lead strategic sales efforts, identify client needs, and partner cross-functionally to deliver tailored solutions supporting regulatory approvals.
Serve as the primary liaison between client and company for all sales-related activities, enhancing visibility and market presence.
Veristat accelerates life-changing therapies to patients worldwide with more than 30 years of expertise. They have a flexible, inclusive culture with 70% remote workforce and 66% women-led teams, having prepared over 105 approved therapies and delivered over 350 rare disease projects.